Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Left anterior descending coronary artery occlusion
5 0 3 0.30 0 0
CUI: C0270985
Disease: Alcohol myopathy
Alcohol myopathy
6 0 3 0.27 0 0
Refractory Chronic Myelogenous Leukemia, BCR-ABL1 Positive
6 0 3 0.27 0 0
CUI: C3888004
Disease: HERMANSKY-PUDLAK SYNDROME 5
HERMANSKY-PUDLAK SYNDROME 5
6 0 3 0.27 0 0
CUI: C1135188
Disease: Critical illness myopathy
Critical illness myopathy
8 0 3 0.23 0 0
CUI: C0476237
Disease: Metabolic symptoms
Metabolic symptoms
9 0 3 0.21 0 0
CUI: C0546483
Disease: Lung cyst
Lung cyst
9 0 3 0.21 0 0
CUI: C1737261
Disease: Acute myeloid leukaemia progression
Acute myeloid leukaemia progression
9 0 3 0.21 0 0
CUI: C0751699
Disease: Minimally Conscious State
Minimally Conscious State
12 0 3 0.18 0 0
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis
18 0 3 0.13 0 0
CUI: C0740985
Disease: Acute anaemia
Acute anaemia
18 0 3 0.13 0 0
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding)
18 0 3 0.13 0 0
CUI: C0023070
Disease: Pharyngolaryngitis
Pharyngolaryngitis
1 0 1 0.12 0 0
CUI: C0154834
Disease: Retinal Microaneurysm
Retinal Microaneurysm
1 0 1 0.12 0 0
Acute posterior multifocal placoid pigment epitheliopathy
1 0 1 0.12 0 0
CUI: C0340648
Disease: dissection of coronary artery
dissection of coronary artery
1 0 1 0.12 0 0
CUI: C0423262
Disease: Corneal endotheliitis
Corneal endotheliitis
1 0 1 0.12 0 0
CUI: C0474354
Disease: Optic disc neovascularization
Optic disc neovascularization
1 0 1 0.12 0 0
CUI: C0521570
Disease: Retinal arteriovenous malformation
Retinal arteriovenous malformation
1 0 1 0.12 0 0
CUI: C0730274
Disease: Vitreomacular traction syndrome
Vitreomacular traction syndrome
1 0 1 0.12 0 0
CUI: C0730275
Disease: Macular pseudohole
Macular pseudohole
1 0 1 0.12 0 0
CUI: C0857406
Disease: Diabetic neovascularization
Diabetic neovascularization
1 0 1 0.12 0 0
CUI: C2931728
Disease: Distal Trisomy 10q Syndrome
Distal Trisomy 10q Syndrome
1 0 1 0.12 0 0
GYRATE ATROPHY OF CHOROID AND RETINA WITH PYRIDOXINE-RESPONSIVE ORNITHINEMIA
1 2 1 0.12 2 5.7E-02
CUI: C4022482
Disease: Chorioretinal hyperpigmentation
Chorioretinal hyperpigmentation
1 0 1 0.12 0 0